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Research 481–510 of 1000+
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- For early diagnosis of young patients with Werner syndrome: Indication for genetic testing
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Biomedical applications of organoids in genetic diseases
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Genetic Variants and Protective Immunity against SARS-CoV-2
- TRPV3 Ion Channel: From Gene to Pharmacology
- Differences in male and female pattern hair loss based on androgens, estrogen, iron, vitamin D, lipid metabolism, and genetic regulation
- Ichthyosis with confetti: clinics, molecular genetics and management
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Congenital atrichia and hypotrichosis
- Darier Sign: A Historical Note
- Skin, Genetic Defects, and Aging
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene